Canonical Allele Identifier: CA276415461
Gene: HBA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1331059
ClinVar RCV Id: RCV001812599
dbSNP Id: rs35431217

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173554A>C , CM000678.2:g.173554A>C GRCh38
NC_000016.9:g.223553A>C , CM000678.1:g.223553A>C GRCh37
NC_000016.8:g.163553A>C NCBI36
NG_000006.1:g.34417A>C
NG_059186.1:g.1904A>C
NG_059271.1:g.5708A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.383A>C MANE Select ENSP00000251595.6:p.Lys128Thr
ENST00000251595.10:c.383A>C ENSP00000251595.6:p.Lys128Thr
ENST00000397806.1:c.287A>C ENSP00000380908.1:p.Lys96Thr
ENST00000482565.1:n.519A>C
NM_000517.4:c.383A>C NP_000508.1:p.Lys128Thr
NM_000517.6:c.383A>C MANE Select NP_000508.1:p.Lys128Thr